Novel nonsense mutation in the SLC12A3 gene in a Spanish case of Gitelman syndrome / Nueva mutación finalizadora en el gen SLC12A3 en un caso de síndrome de Gitelman en España
Nefrología (Madrid)
; 39(1): 108-109, ene.-feb. 2019.
Article
in En
| IBECS
| ID: ibc-181926
Responsible library:
ES1.1
Localization: BNCS
ABSTRACT
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Collection:
06-national
/
ES
Database:
IBECS
Main subject:
Gitelman Syndrome
/
Solute Carrier Family 12, Member 3
/
Mutation
Limits:
Adult
/
Humans
/
Male
Language:
En
Journal:
Nefrología (Madrid)
Year:
2019
Document type:
Article